Drug recall
Allegra Tablets, 60/120mg, 60 count bottles, Rx only, Packaged By Direct Dispensing, Inc., Miami, FL 33147…
FDA recall event 25859 · Class III · Direct Dispensing, Inc.
Key facts
| Event ID | 25859 |
|---|---|
| Recall numbers | D-220-3 |
| Recalling firm | Direct Dispensing, Inc. |
| Product type | Drugs |
| Products | Allegra Tablets, 60/120mg, 60 count bottles, Rx only, Packaged By Direct Dispensing, Inc., Miami, FL 33147, Mfg By Aventis Pharmaceuticals, Kansas City, MO 64137 NDC# 57866-1250-2 |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Mislabeled (by repacker); bottle labeled to contain Allegra actually contains Allegra-D (fexofenadine/pseudoephedrine HCl) |
| Initiation date | Mar 26, 2003 |
| City | Miami |
| Country | United States |
| FEI number | 1052154 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports